NEBIVOLOL
- Product NDC
- 63629-9589
- 11-digit product format
- 636299589
- Labeler code
- 63629
- Product ID
- 63629-9589_3d65f7e0-9bf7-40e1-8744-a626c749b572
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nebivolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212682
- Marketing category
- ANDA
- Marketing start
- 2022-02-14
- Substance
- NEBIVOLOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 030Y90569U | NEBIVOLOL | 118457-14-0 | NEBIVOLOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-9589-1 | 63629958901 | 90 TABLET in 1 BOTTLE (63629-9589-1) | 90 tablet | 2022-12-01 | No | No | Historical |
| 63629-9589-2 | 63629958902 | 30 TABLET in 1 BOTTLE (63629-9589-2) | 30 tablet | 2022-12-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| NEBIVOLOL | Bryant Ranch Prepack | 2024-07-24 | HUMAN PRESCRIPTION DRUG LABEL | 103 |